Package 70518-4480-0

{"route": ["ORAL"], "spl_id": "41ec4523-7a92-5280-e063-6294a90a6942", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312136"], "spl_set_id": ["a1b6a698-f7d9-4adb-9e38-b63e7a85e2b3"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-4480-0)  / 1 TABLET, FILM COATED in 1 POUCH (70518-4480-1)", "package_ndc": "70518-4480-0", "marketing_start_date": "20250913"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4480-2)", "package_ndc": "70518-4480-2", "marketing_start_date": "20251024"}], "brand_name": "OXCARBAZEPINE", "product_id": "70518-4480_41ec4523-7a92-5280-e063-6294a90a6942", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-4480", "generic_name": "OXCARBAZEPINE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXCARBAZEPINE", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "150 mg/1"}], "application_number": "ANDA078069", "marketing_category": "ANDA", "marketing_start_date": "20250913", "listing_expiration_date": "20261231"}